II类MHC分子被活化的B细胞自发内化在酸性内体中。

D A Weber, L B Buck, T M Delohery, N Agostino, B Pernis
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引用次数: 0

摘要

抗体对蛋白质抗原的反应需要B细胞和T细胞之间的特定合作。为了传递辅助信号,在II类MHC的情况下,T细胞必须识别B细胞膜上的加工抗原。加工后的抗原以肽的形式结合在II类MHC分子的给定位点上;为了解决在B细胞中,II类MHC和加工抗原的复合物在哪里形成的问题,我们研究了这两个分子的亚细胞定位。由于这种复合物的形成是抗原加工和呈递的关键步骤,因此这个问题的答案是整个B细胞处理抗原生理学问题的核心。为了收集与这个问题相关的信息,我们比较了B细胞中II类MHC和单价和二价抗免疫球蛋白抗体作为膜免疫球蛋白蛋白配体的细胞内交通。我们通过双色免疫荧光显微镜这样做了,我们已经在lps激活的小鼠B细胞内体中检测到II类MHC分子与免疫球蛋白配体的广泛融合,包括单价和双价。虽然配体可以通过细胞膜内化到达核内体,但II类MHC分子可以通过膜内吞作用或通过靶向新合成的II类MHC分子到达相同的位置。我们收集了II类MHC内吞作用的定量证据,利用荧光活化细胞分选器,荧光化Fab'抗II类MHC在lps活化的小鼠B细胞中的荧光猝灭;这种猝灭表明标签进入了酸性的细胞内腔室。连同其他人用不同方法获得的结果,我们的观察结果支持这样一个概念,即至少在成熟的活化B细胞中,II类MHC分子主要通过内噬途径到达细胞器,在那里它们与加工过的蛋白抗原相遇。由于活化的B细胞内吞其膜II类MHC,而不是膜I类,我们的结果有助于理解B细胞如何将抗原呈递到II类限制性辅助性T细胞,而不是I类限制性细胞溶解性T细胞,这些抗原与膜免疫球蛋白结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Class II MHC molecules are spontaneously internalized in acidic endosomes by activated B cells.

The antibody response to protein antigens requires specific cooperation between B and T cells. In order to deliver the helper signal, T cells must recognize, in the context of Class II MHC, processed antigen on the membrane of B cells. Processed antigen is in the form of peptides bound in a given site of the Class II MHC molecule; in order to address the question of where, in the B cell, the complex of Class II MHC and processed antigen is formed, we studied the subcellular localization of these two molecules. Since the formation of this complex is the crucial step in antigen processing and presentation, the answer to this question is central to the whole problem of the physiology of antigen handling by B cells. To collect information pertinent to the question, we have compared, in B cells, the intracellular traffic of Class II MHC and of monovalent and divalent anti-immunoglobulin antibodies used as protein ligands of the membrane immunoglobulins. We have done so by two-color immunofluorescence microscopy, and we have detected extensive confluence of Class II MHC molecules with the immunoglobulin ligand, both mono- and bi-valent, in the endosomes of LPS-activated murine B cells. Whereas the ligand clearly reaches the endosomes by internalization from the cell membrane, the Class II MHC molecules could reach the same location either by endocytosis from the membrane or through targeting to the endosomes of newly synthesized Class II MHC molecules. We have collected quantitative evidence for endocytosis of Class II MHC by following, with the fluorescence activated cell sorter, the quenching of the fluorescence of fluoresceinated Fab' anti Class II MHC in LPS-activated murine B cells; this quenching indicates the entry of the label into an acidic intracellular compartment. Together with the results of others, obtained with different methods, our observations support the concept that, at least in mature activated B cells, Class II MHC molecules reach the organelles where they meet processed protein antigens, mainly through the endocytic route. Since activated B cells endocytose their membrane Class II MHC, and not their membrane Class I, our results contribute to the understanding of how B cells present antigens, that have bound to their membrane immunoglobulins, to Class II-restricted helper T cells and not to Class I-restricted cytolytic T cells.

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